Open AccessSCN1A gene mutation: A rising cause of human epilepsy syndrome
Author(s) -
Muhammad Akram Choohan,
Ishtiaq Ahmed,
Shahzada Khurram Syed,
Muhammad Naeem
Publication year - 2022
Publication title -
journal of contemporary pharmacy
Language(s) - English
Resource type - Journals
ISSN - 2521-0521
DOI - 10.56770/jcp2022615
Subject(s) - epilepsy , neuroscience , sodium channel , mutation , nervous system , point mutation , gene mutation , epilepsy syndromes , medicine , dravet syndrome , gene , bioinformatics , biology , genetics , chemistry , organic chemistry , sodium